PedAM
Pediatric Disease Annotations & Medicines
| Disease | alport syndrome |
| Phenotype | C0018784|sensorineural hearing loss |
| Sentences | 1 |
| PubMedID- 22887808 | There were two deafness genes on xq22.3; col4a5 which is implicated in alport syndrome with variable sensorineural hearing loss [barker et al., 1990] and prps1 which is mutated in non-syndromic x-linked deafness-1 [liu et al., 2010]. |
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